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倍半萜 germacrone:一种具有多靶点的倍半萜,具有有前景的抗癌和慢性病应用。

Germacrone: A Multi-targeting Sesquiterpene with Promising Anti-cancer and Chronic Disease Applications.

机构信息

University Institute of Pharma Sciences, Chandigarh University, Gharuan, Mohali, Punjab, India.

Department of Pharmaceutical Chemistry, Guru Gobind Singh College of Pharmacy, Yamuna Nagar, Haryana, India.

出版信息

Anticancer Agents Med Chem. 2024;24(19):1396-1406. doi: 10.2174/0118715206312324240805075050.

DOI:10.2174/0118715206312324240805075050
PMID:39113300
Abstract

BACKGROUND

Germacrone, a naturally occurring active compound found in essential oils extracted from medicinal plants within the Zingiberaceae family, has garnered attention for its potential therapeutic applications. Extensive research has highlighted its multi-targeting capabilities, positioning it as a promising treatment for various chronic diseases, including cancer, cardiovascular conditions, and neurodegenerative disorders like Alzheimer's disease.

OBJECTIVE

This review aims to provide a comprehensive overview of germacrone as a scaffold for developing multi-targeting drugs with therapeutic potential against a range of chronic disorders. The study delves into the molecular mechanisms that underlie the therapeutic effects of germacrone and explores its potential targets, including NF-κB, PI3K/AKT/mTOR, p53, JAK/STAT, caspase, apoptosis, and autophagy induction.

METHODS

A systematic review of literature databases was conducted to gather relevant studies on germacrone and its therapeutic applications. The molecular mechanisms and potential targets of germacrone were examined to elucidate its multi-targeting capabilities.

RESULTS

Germacrone exhibits significant potential in the management of chronic diseases, with demonstrated effects on various cellular pathways. The review highlights its impact on NF-κB, PI3K/AKT/mTOR, p53, JAK/STAT, caspase, apoptosis, and autophagy induction, showcasing its versatility in targeting multiple pathways associated with chronic conditions. Germacrone has emerged as a promising candidate for the treatment of diverse chronic diseases. The understanding of its multi-targeting capabilities, coupled with its natural origin, positions it as a valuable scaffold for developing therapeutics.

CONCLUSION

The exploration of germacrone as a structural framework for multi-targeting drugs offers a potential avenue to enhance efficacy while minimizing potential side effects. Further research and clinical trials are warranted to validate the therapeutic potential of germacrone in diverse medical contexts.

摘要

背景

倍半萜烯,一种天然存在的活性化合物,存在于姜科药用植物提取的精油中,因其潜在的治疗应用而受到关注。广泛的研究强调了它的多靶点作用,使其成为治疗各种慢性疾病的有前途的药物,包括癌症、心血管疾病和阿尔茨海默病等神经退行性疾病。

目的

本综述旨在提供倍半萜烯作为开发具有治疗多种慢性疾病潜力的多靶点药物的支架的全面概述。研究深入探讨了倍半萜烯治疗作用的分子机制,并探讨了其潜在的靶点,包括 NF-κB、PI3K/AKT/mTOR、p53、JAK/STAT、半胱天冬酶、细胞凋亡和自噬诱导。

方法

对文献数据库进行系统综述,以收集有关倍半萜烯及其治疗应用的相关研究。检查了倍半萜烯的分子机制和潜在靶点,以阐明其多靶点作用。

结果

倍半萜烯在慢性疾病的管理中具有显著的潜力,对各种细胞途径表现出明显的效果。综述强调了其对 NF-κB、PI3K/AKT/mTOR、p53、JAK/STAT、半胱天冬酶、细胞凋亡和自噬诱导的影响,展示了其在靶向与慢性疾病相关的多种途径方面的多功能性。倍半萜烯已成为治疗多种慢性疾病的有希望的候选药物。对其多靶点作用的认识,加上其天然来源,使其成为开发治疗药物的有价值的支架。

结论

探索倍半萜烯作为多靶点药物的结构框架为提高疗效同时最小化潜在副作用提供了潜在途径。需要进一步的研究和临床试验来验证倍半萜烯在不同医学背景下的治疗潜力。

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Germacrone: A Multi-targeting Sesquiterpene with Promising Anti-cancer and Chronic Disease Applications.倍半萜 germacrone:一种具有多靶点的倍半萜,具有有前景的抗癌和慢性病应用。
Anticancer Agents Med Chem. 2024;24(19):1396-1406. doi: 10.2174/0118715206312324240805075050.
2
Germacrone exerts anti-cancer effects on gastric cancer through induction of cell cycle arrest and promotion of apoptosis.倍半萜Germacrone 通过诱导细胞周期停滞和促进细胞凋亡对胃癌发挥抗癌作用。
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Germacrone protects against oxygen-glucose deprivation/reperfusion injury by inhibiting autophagy processes in PC12 cells.倍半萜烯通过抑制 PC12 细胞自噬过程来防止氧葡萄糖剥夺/再灌注损伤。
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本文引用的文献

1
Germacrone, isolated from Curcuma wenyujin, inhibits melanin synthesis through the regulation of the MAPK signaling pathway.莪术醇从温郁金中分离得到,通过调节 MAPK 信号通路抑制黑色素合成。
J Nat Med. 2024 Sep;78(4):863-875. doi: 10.1007/s11418-024-01818-x. Epub 2024 May 29.
2
Germacrone alleviates breast cancer-associated osteolysis by inhibiting osteoclastogenesis via inhibition of MAPK/NF-κB signaling pathways.倍半萜烯通过抑制 MAPK/NF-κB 信号通路抑制破骨细胞生成来缓解乳腺癌相关性溶骨性骨病。
Phytother Res. 2024 Jun;38(6):2860-2874. doi: 10.1002/ptr.8195. Epub 2024 Apr 1.
3
Integrated 16S rRNA sequencing and metabolomic analysis reveals the potential protective mechanism of Germacrone on diabetic nephropathy in mice.
整合 16S rRNA 测序和代谢组学分析揭示了姜酮对糖尿病肾病小鼠的潜在保护机制。
Acta Biochim Biophys Sin (Shanghai). 2024 Mar 25;56(3):414-426. doi: 10.3724/abbs.2024021.
4
Germacrone, A Novel and Safe Anticancer Agent from Genus : A Review of its Mechanism.莪术醇,一种新型安全抗癌药物,来自莪术属:作用机制综述。
Anticancer Agents Med Chem. 2023;23(13):1490-1498. doi: 10.2174/1871520623666230420094628.
5
Novel Estrogen Receptor-Targeted Agents for Breast Cancer.新型雌激素受体靶向药物治疗乳腺癌。
Curr Treat Options Oncol. 2023 Jul;24(7):821-844. doi: 10.1007/s11864-023-01079-y. Epub 2023 May 2.
6
Neuroprotective effect of transient receptor potential Vanilloid 1 agonist capsaicin in Alzheimer's disease model induced with okadaic acid.辣椒素作为瞬时受体电位香草素 1 激动剂对岗田酸诱导阿尔茨海默病模型的神经保护作用。
Int Immunopharmacol. 2023 May;118:109925. doi: 10.1016/j.intimp.2023.109925. Epub 2023 Apr 1.
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The interaction between ferroptosis and inflammatory signaling pathways.铁死亡与炎症信号通路的相互作用。
Cell Death Dis. 2023 Mar 21;14(3):205. doi: 10.1038/s41419-023-05716-0.
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Cell Commun Signal. 2023 Mar 14;21(1):61. doi: 10.1186/s12964-023-01077-5.
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The function of natural compounds in important anticancer mechanisms.天然化合物在重要抗癌机制中的作用。
Front Oncol. 2023 Jan 4;12:1049888. doi: 10.3389/fonc.2022.1049888. eCollection 2022.
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